Canonical Allele Identifier: PA2829436979
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Glu13376Gly
CA237855
NM_003319.4:c.40127A>G